Product information
From Health Canada
The product monograph is developed by a drug sponsor according to guidelines published by Health Canada that provide direction on the content and format. The veterinary labelling is developed by the drug sponsor according to the Food and Drug Regulations. While Health Canada reviews the product monograph or the veterinary labelling as part of the drug review process, it remains the responsibility of the drug sponsor to ensure that the product monograph or the veterinary labelling is complete and accurate.
Current status:
Marketed
Current status date:
2021-07-29
Original market date: See footnote 1
1997-10-27
Product name:
FEIBA NF
Description:
700 TO 1300 UNITS/VIAL & 20 ML DILUENT
DIN:
02202581
Product Monograph/Veterinary Labelling:
Date:
2020-12-29
Product monograph/Veterinary Labelling (PDF version ~ 175K)
Company:
TAKEDA CANADA INC
3800
22 Adelaide Street West
Toronto
Ontario
Canada
M5H 4E3
Class:
Human
Dosage form(s):
Powder For Solution , Kit
Route(s) of administration:
Intravenous
Number of active ingredient(s):
1
Schedule(s):
Schedule D
American Hospital Formulary Service (AHFS): See footnote 3
20:28.16
Anatomical Therapeutic Chemical (ATC): See footnote 4
B02BD03 FACTOR VIII INHIBITOR BYPASSING ACTIVITY
Active ingredient group (AIG) number:See footnote5
0133136002
| Active ingredient(s) | Strength |
|---|---|
| ANTI-INHIBITOR COAGULANT COMPLEX | 1300 UNIT / VIAL |
Risk Management Plans See footnote 7
A Risk Management Plan (RMP) for this product was submitted.